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结肠癌中δ样配体4(Dll4)的表达及缺氧标志物

Expression of delta-like ligand 4 (Dll4) and markers of hypoxia in colon cancer.

作者信息

Jubb A M, Turley H, Moeller H C, Steers G, Han C, Li J-L, Leek R, Tan E Y, Singh B, Mortensen N J, Noguera-Troise I, Pezzella F, Gatter K C, Thurston G, Fox S B, Harris A L

机构信息

Nuffield Department of Clinical Laboratory Sciences, University of Oxford, John Radcliffe Hospital, Headington, Oxford OX3 9DS, UK.

出版信息

Br J Cancer. 2009 Nov 17;101(10):1749-57. doi: 10.1038/sj.bjc.6605368. Epub 2009 Oct 20.

Abstract

BACKGROUND

Delta-like ligand 4 (Dll4) is a Notch ligand that is upregulated by hypoxia and vascular endothelial growth factor-A (VEGF-A) and is reported to have a role in tumor angiogenesis. Evidence from xenograft studies suggests that inhibiting Dll4-Notch signalling may overcome resistance to anti-VEGF therapy. The aim of this study was to characterise the expression of Dll4 in colon cancer and to assess whether it is associated with markers of hypoxia and prognosis.

METHOD

In all, 177 colon cancers were represented in tissue microarrays. Immunohistochemistry was performed using validated antibodies against Dll4, VEGF, hypoxia-inducible factor (HIF)-1alpha, HIF-2alpha, prolyl hydroxylase (PHD)1, PHD2, PHD3 and carbonic anhydrase 9 (CA9).

RESULTS

The expression of Dll4 was observed preferentially in the endothelium of 71% (125 out of 175) of colon cancers, but not in the endothelium adjacent to normal mucosa (none out of 107, P<0.0001). The expression of VEGF was significantly associated with HIF-2alpha (P<0.0001) and Dll4 (P=0.010). Only HIF-2alpha had a significant multivariate prognostic effect (hazard ratio 1.61, 95% confidence interval 1.01-2.57). Delta-like ligand 4 was also expressed by neoplastic cells, particularly neoplastic goblet cells.

CONCLUSION

Endothelial expression of Dll4 is not a prognostic factor, but is significantly associated with VEGF. Assessing endothelial Dll4 expression may be critical in predicting response to anti-VEGF therapies.

摘要

背景

Delta样配体4(Dll4)是一种Notch配体,受缺氧和血管内皮生长因子-A(VEGF-A)上调,据报道在肿瘤血管生成中起作用。异种移植研究的证据表明,抑制Dll4-Notch信号传导可能克服对抗VEGF治疗的耐药性。本研究的目的是表征Dll4在结肠癌中的表达,并评估其是否与缺氧标志物和预后相关。

方法

总共177例结肠癌组织被制作成组织芯片。使用针对Dll4、VEGF、缺氧诱导因子(HIF)-1α、HIF-2α、脯氨酰羟化酶(PHD)1、PHD2、PHD3和碳酸酐酶9(CA9)的经过验证的抗体进行免疫组织化学检测。

结果

在71%(175例中的125例)的结肠癌内皮中观察到Dll4的表达,但在正常黏膜相邻的内皮中未观察到(107例中无表达,P<0.0001)。VEGF的表达与HIF-2α(P<0.0001)和Dll4(P=0.010)显著相关。只有HIF-2α具有显著的多因素预后效应(风险比1.61,95%置信区间1.01-2.57)。Delta样配体4也由肿瘤细胞表达,特别是肿瘤杯状细胞。

结论

Dll4的内皮表达不是一个预后因素,但与VEGF显著相关。评估内皮Dll4表达可能对预测抗VEGF治疗的反应至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/935f/2778546/d79cd2bc5200/6605368f1.jpg

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